Hydrochloric Acid → HCID 68607770, compound

HRID 732507Notes

Reaction equation

HRID 732507 reaction equation
[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:13]=[C:12]([S:14](Cl)(=[O:16])=[O:15])[CH:11]=[C:6]([C:7]([O:9]C)=[O:8])[CH:5]=1.[CH3:19][NH:20][CH3:21].[OH-].[Na+].Cl>C1COCC1.C(OCC)(=O)C.CO>[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:13]=[C:12]([S:14](=[O:16])(=[O:15])[N:20]([CH3:21])[CH3:19])[CH:11]=[C:6]([C:7]([OH:9])=[O:8])[CH:5]=1

Participants

8

Procedure

Dissolve commercially available 5-chlorosulfonyl-isophthalic acid dimethyl ester (422 mg, 1.43 mmol) in THF (10 mL) and add dimethylamine (2.0 M in THF, 2.5 mL, 5 mmol). Stir at room temperature 3 h, dilute with ethyl acetate, wash with 10% aqueous potassium carbonate, 0.1 N citric acid and saturated aqueous sodium chloride. Dry (magnesium sulfate), filter and concentrate. Dissolve the residue in acetone (10 mL) and methanol (5 mL). Add a solution of NaOH (60 mg, 1.43 mmol) in methanol (0.7 mL). Stir at room temperature 16 h and acidify with 1 N HCl to about pH=1. Partition between ethyl acetate and water, dry (magnesium sulfate) and concentrate to give the title compound.

Workup

  1. washwash with 10% aqueous potassium carbonate, 0.1 N citric acid and saturated aqueous sodium chloride
  2. dry with materialDry (magnesium sulfate)
  3. filtrationfilter
  4. concentrationconcentrate
  5. dissolutionDissolve the residue in acetone (10 mL)
  6. stirringStir at room temperature 16 h
  7. customPartition between ethyl acetate and water
  8. dry with materialdry (magnesium sulfate)
  9. concentrationconcentrate

Sources & evidence

ORD record
ord-d185c0662af6418eb20d9fc77049ceaf
Source dataset
uspto-grants-2009_09
Patent number
US07585885B2

Reaction notes

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